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在模拟因兴奋剂检查目的而摄入受污染产品的研究中,对选择性雄激素受体调节剂S-23的尿液代谢物消除情况的调查。

Investigations Into the Urinary Metabolite Elimination Profile of the Selective Androgen Receptor Modulator S-23 in Studies Mimicking Contaminated Product Ingestion for Doping Control Purposes.

作者信息

Alhalabi Hana, Korsmeier Linus, Thomas Andreas, Thevis Mario

机构信息

Center for Preventive Doping Research, Institute of Biochemistry, German Sport University Cologne, Cologne, Germany.

European Monitoring Center for Emerging Doping Agents (EUMoCEDA), Cologne, Germany.

出版信息

Biomed Chromatogr. 2025 Jun;39(6):e70090. doi: 10.1002/bmc.70090.

DOI:10.1002/bmc.70090
PMID:40277337
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12023825/
Abstract

Selective androgen receptor modulators (SARMs) have repeatedly been reason of adverse analytical findings (AAFs) in routine doping controls. Among these, S-23 has been identified in five AAFs reported in 2022. In addition to intentional doping, inadvertent exposure through contaminated dietary supplements has emerged as a significant concern, purportedly as well as evidently contributing to AAFs involving SARMs. Thus, the differentiation of inadvertent intake and intentional abuse of S-23 is of growing relevance. This study aimed at investigating the urinary concentration profile of microdosed S-23 and to characterize the elimination pattern. Single and multidose administration studies with 1, 10, and 50 μg of S-23 were conducted, and collected urine samples were analyzed by LC-MS/MS following enzymatic hydrolysis and solid-phase extraction. The analytical method was validated for a semiquantitative detection of S-23 and characterized by a limit of detection of 1 pg/mL. A total of 18 metabolites was detected in human in vivo samples following oral administration of microdosed S-23. Moreover, the study demonstrated that a single dose of 1 μg can be detected for an average of up to 253 h, while a single dose of 50 μg can be detected up to 544 h on average.

摘要

选择性雄激素受体调节剂(SARMs)多次成为常规兴奋剂检测中出现不利分析结果(AAFs)的原因。其中,S-23在2022年报告的5例AAFs中被检测到。除了故意使用兴奋剂外,通过受污染的膳食补充剂意外接触也已成为一个重大问题,据称这显然也是导致涉及SARMs的AAFs的原因。因此,区分S-23的意外摄入和故意滥用变得越来越重要。本研究旨在调查微剂量S-23的尿液浓度分布,并表征其消除模式。进行了1、10和50μg S-23的单剂量和多剂量给药研究,收集的尿液样本在酶水解和固相萃取后通过液相色谱-串联质谱(LC-MS/MS)进行分析。该分析方法经验证可用于S-23的半定量检测,检测限为1pg/mL。口服微剂量S-23后,在人体体内样本中总共检测到18种代谢物。此外,研究表明,1μg的单剂量平均可检测长达253小时,而50μg的单剂量平均可检测长达544小时。

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本文引用的文献

1
In Vitro and In Vivo Human Metabolism of Ostarine, a Selective Androgen Receptor Modulator and Doping Agent.奥沙他汀的人体体外和体内代谢研究,一种选择性雄激素受体调节剂和兴奋剂。
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Detection of the selective androgen receptor modulator S-23 and its metabolites in equine urine and plasma following oral administration.口服给药后马尿液和血浆中选择性雄激素受体调节剂S-23及其代谢物的检测。
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Selective androgen receptor modulator use and related adverse events including drug-induced liver injury: Analysis of suspected cases.
选择性雄激素受体调节剂的使用及相关不良事件,包括药物性肝损伤:疑似病例分析。
Eur J Clin Pharmacol. 2024 Feb;80(2):185-202. doi: 10.1007/s00228-023-03592-3. Epub 2023 Dec 7.
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In vitro characterization of S-23 metabolites produced by human liver microsomes, and subsequent application to urine after a controlled oral administration.人肝微粒体产生的 S-23 代谢物的体外特征分析,以及随后在口服给予药物后的尿液中的应用。
J Pharm Biomed Anal. 2022 Apr 1;212:114660. doi: 10.1016/j.jpba.2022.114660. Epub 2022 Feb 15.
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Investigations into the elimination profiles and metabolite ratios of micro-dosed selective androgen receptor modulator LGD-4033 for doping control purposes.为兴奋剂控制目的而对微剂量选择性雄激素受体调节剂 LGD-4033 的消除谱和代谢物比值进行研究。
Anal Bioanal Chem. 2022 Jan;414(2):1151-1162. doi: 10.1007/s00216-021-03740-7. Epub 2021 Nov 4.
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Analysis of the growing public interest in selective androgen receptor modulators.分析公众对选择性雄激素受体调节剂日益增长的兴趣。
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